US7531158B2ExpiredUtilityA1

Vapor phase synthesis of double-walled carbon nanotubes

Assignee: LEE CHEOL JINPriority: Mar 20, 2003Filed: Mar 17, 2004Granted: May 12, 2009
Est. expiryMar 20, 2023(expired)· nominal 20-yr term from priority
Inventors:Cheol Jin Lee
C01B 32/162B82Y 30/00B82Y 40/00C01B 2202/04
52
PatentIndex Score
1
Cited by
13
References
7
Claims

Abstract

A method of massively synthesizing double-walled carbon nanotubes is provided. In the method, catalyst metal particles having a size of a few nanometers are embedded in nano pores of a support material powder. Then, the support material powder embedding the catalyst metal particles is sintered at a temperature of 700-900° C. Then, the support material powder embedding the catalyst metal particles is loaded in a reactor. Thereafter, high purity double-walled carbon nanotubes are formed massively by vaporizing a carbon source solution at a temperature of 700-1100° C. and supplying the vaporized carbon source gas, or by directly supplying a carbon source gas to the reactor.

Claims

exact text as granted — not AI-modified
1. A method of synthesizing double-walled carbon nanotubes, the method comprising:
 embedding catalyst metal particles composed of Fe, Co, Ni, Mo or an alloy of the elements and having a size of 2-5 nm in nano pores of a support material powder composed of MgO, Al 2 O 3 , zeolite or silica; 
 sintering the support material powder in which the catalyst metal particles are embedded; and 
 forming the double-walled carbon nanotubes by supplying a carbon source gas to the catalyst metal particles embedded in the support material powder and reacting the carbon source gas with the catalyst metal particles. 
 
     
     
       2. The method of  claim 1 , wherein the embedding the catalyst metal particles in the nano pores of the support material powder comprises:
 making a first solution including the catalyst metal particles; 
 mixing the first solution with the support material powder to form a second solution; 
 removing moisture included in the second solution; and 
 pulverizing the support material powder including the catalyst metal particles to form the support material powder in which the catalyst metal particles are supported. 
 
     
     
       3. The method of  claim 2 , wherein the removing the moisture is performed by a vacuum oven for 15 hours at a temperature of 150° C. 
     
     
       4. The method of  claim 2 , wherein if the second solution is a solution containing Fe, Ni or Co, Mo, and MgO, a molar ratio of Fe, Ni or Co:Mo:MgO is 0.7-1:0.1-0.3:10-13,
 if the second solution is a solution containing Fe or Ni, Mo, and MgO, a molar ratio of Fe:Ni:Mo:MgO is 0.7-1:0.1-0.3:0.1-0.3:10-13, and 
 if the second solution is a solution containing Fe or Co, Mo, and MgO, a molar ratio of Fe:Co:Mo:MgO is 0.7-1:0.1-0.3:0.1-0.3:10-13. 
 
     
     
       5. The method of  claim 1 , wherein the sintering is performed in air atmosphere for 6-12 hours at a temperature of 700-900° C. 
     
     
       6. The method of  claim 1 , wherein the forming the double-walled carbon nanotubes comprises:
 loading the support material powder embedding the catalyst metal particles in a reactor; 
 maintaining the temperature of the reactor including the support material powder at 700-1100° C.; and 
 supplying a carbon source solution selected from the group consisting of alcohol, benzene, hexane, THF (tetra hydrofuran) and propanol, to an inside of the reactor in a gas form using an evaporator. 
 
     
     
       7. The method of  claim 1 , wherein the forming the double-walled carbon nanotubes comprises:
 loading the support material powder embedding the catalyst metal particles in a reactor; 
 maintaining the temperature of the reactor including the support material powder at 700-1100° C.; and 
 supplying a carbon source gas selected from the group consisting of acetylene, methane, ethylene, propane and CO to an inside of the reactor.

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